1,3-디옥살란

1,3-디옥살란
1,3-디옥살란 구조식 이미지
카스 번호:
646-06-0
한글명:
1,3-디옥살란
동의어(한글):
1,3-다이옥솔레인;1,3-디옥살란;1,3-디옥소란;디옥살란1,3;다이옥솔레인
상품명:
1,3-Dioxolane
동의어(영문):
Dioxolane;Dioxolan;1,3-Dioxolan;1,3-Dioxalane;1,3-Dioxlane;1,3-DioxoL;1,3-DIOXACYCLOPENTANE;Dioxlane;dioxolanne;glycoformal
CBNumber:
CB5712494
분자식:
C3H6O2
포뮬러 무게:
74.08
MOL 파일:
646-06-0.mol
MSDS 파일:
SDS

1,3-디옥살란 속성

녹는점
-95 °C (lit.)
끓는 점
75-76 °C/1.013 hPa
밀도
1.06 g/mL at 25 °C (lit.)
증기 밀도
2.6 (vs air)
증기압
70 mm Hg ( 20 °C)
굴절률
n20/D 1.401(lit.)
인화점
35 °F
저장 조건
Store at <= 20°C.
용해도
1000g/l 가용성
물리적 상태
액체
색상
흰색에서 황백색까지
폭발한계
2.1-20.5%(V)
수용성
녹는
BRN
102453
노출 한도
ACGIH: TWA 20 ppm
안정성
4°C 이하
InChIKey
WNXJIVFYUVYPPR-UHFFFAOYSA-N
LogP
-0.37 at 20℃
CAS 데이터베이스
646-06-0(CAS DataBase Reference)
NIST
1,3-Dioxolane(646-06-0)
EPA
1,3-Dioxolane (646-06-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F
위험 카페고리 넘버 11
안전지침서 16
유엔번호(UN No.) UN 1166 3/PG 2
WGK 독일 1
RTECS 번호 JH6760000
자연 발화 온도 525 °F
TSCA Yes
위험 등급 3
포장분류 II
HS 번호 29329970
유해 물질 데이터 646-06-0(Hazardous Substances Data)
독성 LD50 orally in Rabbit: 3000 mg/kg LD50 dermal Rabbit 9074 mg/kg
기존화학 물질 KE-12027
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H225 고인화성 액체 및 증기 인화성 액체 구분 2 위험 GHS hazard pictograms P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H360 태아 또는 생식능력에 손상을 일으킬 수 있음 생식독성 물질 구분 1A, 1B 위험 GHS hazard pictograms
예방조치문구:
P201 사용 전 취급 설명서를 확보하시오.
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
NFPA 704
3
1 2

1,3-디옥살란 MSDS


Ethylene glycol methylene ether

1,3-디옥살란 C화학적 특성, 용도, 생산

화학적 성질

Colourless Liquid. Miscible with water, soluble in alcohol, ether and benzene. The azeotrope formed with water, the azeotrope is 70-73°C, and the water content is 6.7%. Decolorize bromine water.

용도

1,3-Dioxolane is an intermediate for the preparation of Acyclovir (A192400). Also, 1,3-Dioxolane is used in the synthesis of new Vandetanib (V097100) analogs.

주요 응용

1,3-Dioxolane (DOXL) is a cyclic ether. It is a green solvent. It undergoes reaction with C60 to afford an epoxide and 1,3-dioxolane derivative. Reaction has been reported to proceed via a diradical mechanism. A mixture of tetra(ethylene glycol) dimethyl ether (TEGDME) and DOXL has been used to compose the binary electrolyte for use in lithium-sulfur battery. Its efficacy as a solvent in a non-aqueous redox flow battery system has been tested. 1,3-Dioxolane may be used in the fabrication of batteries and capacitors. It may be used as one of the co-solvent to prepare the electrolyte for lithium-sulfur batteries.

정의

ChEBI: 1,3-dioxolane is a cyclic acetal that is pentane in which the carbon atoms at positions 1 and 3 are replaced by oxygen atoms respectively. It is a dioxolane and a cyclic acetal.

일반 설명

A clear colorless liquid. Flash point 35°F. Slightly denser than water. Vapors heavier than air.

공기와 물의 반응

Highly flammable. When exposed to air 1,3-Dioxolane undergoes autooxidation with formation of peroxides. In the distillation process peroxides will concentrate causing violent explosion. Soluble in water.

반응 프로필

Ethers, such as 1,3-Dioxolane, can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

건강위험

The acute inhalation and oral toxicity of1,3-dioxolane is low in test animals. Thevapor is irritant to eyes and respiratory tract.Application of the liquid produced severeirritation in rabbits’ eyes and mild action onthe animals’ skin. The information on thetoxicity of this compound in humans is notknown.
The inhalation LC50 value of 4-hour exposurein rats is in the range of 20,000 mg/m3,and the oral LD50 is 3000 mg/kg (NIOSH1986).

화재위험

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

공업 용도

1,3-Dioxolane is used to dissolve a wide spectrum of polymeric materials such as acrylates, alkyds, cellulosics, epoxies, polycarbonates, polyesters, urethanes, and vinyl resins. In many cases, 1,3-dioxolane solvent can replace the chlorinated solvents that were used previously to dissolve many of these polymers. The excellent solvency of 1,3-dioxolane for polymeric compositions makes this cyclic ether a valuable component in paint remover formulations. 1,3-Dioxolane is used to treat polyester fibers for improved dye retention, application of cross-linking agents to cellulosic fibers, and bonding of acrylonitrile polymers. 1,3-Dioxolane is used in metal working and electroplating formulations, as a complexing solvent for organometallic and inorganic salts, and in the preparation of lithium battery electrolyte solutions. 1,3-Dioxolane is a valuable reactant in the polymerization reactions to produce polyacetals. Polymerization reactions of dioxolane with itself or with aldehydes and ethers are catalyzed by a Lewis acid to yield the polyacetal polymers. The methylene group (CH2) bonded to the two oxygen atoms in dioxolane is susceptible to radical abstraction of a hydrogen atom and the resultant dioxolane radical species can be added across various double bond configurations.

Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. Mildly toxic by skin contact and inhalation. A shin and severe eye irritant. Mutation data reported. A very dangerous fire hazard when exposed to heat or flame; can react with oxidizers. Used in lithium batteries. Potentially explosive reaction with lithium perchlorate. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Dry it with solid NaOH, KOH or CaSO4, and distil it from sodium or sodium amalgam. Barker et al. [J Chem Soc 802 1959] heated 34mL of dioxalane under reflux with 3g of PbO2 for 2hours, then cooled and filtered. After adding xylene (40mL) and PbO2 (2g) to the filtrate, the mixture is fractionally distilled. Addition of xylene (20mL) and sodium wire to the main fraction (b 70-71o) led to a vigorous reaction, following which the mixture was again fractionally distilled. Xylene and sodium additions are made to the main fraction (b 73-74o) before it is finally distilled. [Beilstein 19/1 V 6.]

1,3-디옥살란 준비 용품 및 원자재

원자재

준비 용품


1,3-디옥살란 공급 업체

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